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151名健康日本受试者中硫嘌呤S-甲基转移酶突变等位基因(TPMT*2、*3A、*3B和*3C)的频率以及一名先证者家族中TPMT*3C的遗传情况。

Frequencies of thiopurine S-methyltransferase mutant alleles (TPMT*2, *3A, *3B and *3C) in 151 healthy Japanese subjects and the inheritance of TPMT*3C in the family of a propositus.

作者信息

Kubota T, Chiba K

机构信息

Research Testing Department, SRL, Inc., Hachioji-shi, Tokyo, Japan.

出版信息

Br J Clin Pharmacol. 2001 May;51(5):475-7. doi: 10.1046/j.1365-2125.2001.01371.x.

DOI:10.1046/j.1365-2125.2001.01371.x
PMID:11422006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2014472/
Abstract

AIMS

To determine the frequencies of four thiopurine S-methyltransferase (TPMT) mutant alleles, TPMT*2, *3A, *3B and *3C in a normal Japanese population.

METHODS

Genotypes were determined in 151 Japanese subjects and in six family members of a propositus using polymerase chain reaction (PCR)-restriction fragment length polymorphism and allele-specific PCR assays.

RESULTS

Only one TPMT3C heterozygote was identified (gene frequency 0.3%). TPMT2, *3A and 3B were not detected. In addition, TPMT3C was found to have been inherited from the mother and passed on to the son of the propositus.

CONCLUSIONS

TPMT*3C appears to be most prevalent among the known mutant allele of TPMT in a Japanese population which may have some relevance for the treatment of Japanese patients with thiopurine drugs.

摘要

目的

确定正常日本人群中四种硫嘌呤甲基转移酶(TPMT)突变等位基因TPMT*2、*3A、3B和3C的频率。

方法

采用聚合酶链反应(PCR)-限制性片段长度多态性和等位基因特异性PCR检测法,对151名日本受试者及一名先证者的六名家庭成员进行基因分型。

结果

仅鉴定出一名TPMT3C杂合子(基因频率0.3%)。未检测到TPMT2、3A和3B。此外,发现TPMT*3C是从母亲遗传而来,并传递给了先证者的儿子。

结论

在日本人群中,TPMT*3C似乎是TPMT已知突变等位基因中最常见的,这可能与日本硫嘌呤类药物治疗患者有关。

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本文引用的文献

1
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Biol Pharm Bull. 2000 Sep;23(9):1090-3. doi: 10.1248/bpb.23.1090.
2
Genetic analysis of thiopurine methyltransferase polymorphism in a Japanese population.日本人群中硫嘌呤甲基转移酶多态性的遗传分析。
Mutat Res. 2000 Mar 14;448(1):91-5. doi: 10.1016/s0027-5107(00)00004-x.
3
Thiopurine methyltransferase genotype and the toxicity of azathioprine in Japanese.硫嘌呤甲基转移酶基因型与硫唑嘌呤在日本人中的毒性。
Intern Med. 1999 Dec;38(12):944-7. doi: 10.2169/internalmedicine.38.944.
4
The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations.白种人和亚洲人群中硫嘌呤甲基转移酶等位基因的频率及分布。
Pharmacogenetics. 1999 Feb;9(1):37-42. doi: 10.1097/00008571-199902000-00006.
5
Polymorphism of the thiopurine S-methyltransferase gene in African-Americans.非裔美国人中硫嘌呤甲基转移酶基因的多态性。
Hum Mol Genet. 1999 Feb;8(2):371-6. doi: 10.1093/hmg/8.2.371.
6
Thiopurine methyltransferase alleles in British and Ghanaian populations.英国和加纳人群中的硫嘌呤甲基转移酶等位基因。
Hum Mol Genet. 1999 Feb;8(2):367-70. doi: 10.1093/hmg/8.2.367.
7
Genotypic and phenotypic analysis of the polymorphic thiopurine S-methyltransferase gene (TPMT) in a European population.欧洲人群中多态性硫嘌呤甲基转移酶基因(TPMT)的基因型和表型分析。
Br J Pharmacol. 1998 Oct;125(4):879-87. doi: 10.1038/sj.bjp.0702152.
8
Detection of known and new mutations in the thiopurine S-methyltransferase gene by single-strand conformation polymorphism analysis.通过单链构象多态性分析检测硫嘌呤S-甲基转移酶基因中的已知和新突变。
Hum Mutat. 1998;12(3):177-85. doi: 10.1002/(SICI)1098-1004(1998)12:3<177::AID-HUMU5>3.0.CO;2-E.
9
Human thiopurine methyltransferase pharmacogenetics. Kindred with a terminal exon splice junction mutation that results in loss of activity.人类硫嘌呤甲基转移酶药物遗传学。家系中有导致活性丧失的末端外显子剪接连接突变。
J Clin Invest. 1998 Mar 1;101(5):1036-44. doi: 10.1172/JCI1004.
10
Human thiopurine methyltransferase pharmacogenetics: gene sequence polymorphisms.
Clin Pharmacol Ther. 1997 Jul;62(1):60-73. doi: 10.1016/S0009-9236(97)90152-1.